International safety notice

Cascadia Interbody System

Swiss / SwissMedic · CHE · Apr 30, 2018

Key facts

Title Cascadia Interbody System
Regulator Swiss / SwissMedic
Country CHE
Brand Cascadia Interbody System
Manufacturer K2M Inc.
Models 2121408CL7‐G2, 6101‐2226012LL8‐G2, 6101‐2225014LP‐G2, 6101‐2225516LL8‐, 6101‐2121407CL7‐G2, 6101‐2225016LL8‐, 6101‐2226016LL8‐G2, GACG‐29761, 2018‐04‐20, 20.04.2018verwendeteMenge, 6101‐2226008LP‐G2, 12x14x11 and 99 more
Event type Safety Notice
Date Apr 30, 2018
Regulator page fsca.swissmedic.ch

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 Matching device models in FDA data
  • 1–9 Matching catalog numbers in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices